CN115043768A - Method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl - Google Patents
Method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl Download PDFInfo
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- 238000007142 ring opening reaction Methods 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title claims abstract description 34
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 title claims abstract description 26
- 230000002194 synthesizing effect Effects 0.000 title claims abstract description 19
- 238000006243 chemical reaction Methods 0.000 claims abstract description 29
- 239000002253 acid Substances 0.000 claims abstract description 14
- 230000001737 promoting effect Effects 0.000 claims abstract description 13
- 150000001263 acyl chlorides Chemical class 0.000 claims abstract description 7
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 6
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 4
- 239000012298 atmosphere Substances 0.000 claims abstract description 3
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000002808 molecular sieve Substances 0.000 claims description 8
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000001072 heteroaryl group Chemical group 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 230000008569 process Effects 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 239000000758 substrate Substances 0.000 abstract description 9
- 238000001308 synthesis method Methods 0.000 abstract description 5
- -1 amidine compound Chemical class 0.000 abstract description 4
- 125000000524 functional group Chemical group 0.000 abstract description 3
- 238000002360 preparation method Methods 0.000 description 20
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 10
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 9
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000001939 inductive effect Effects 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- JMVIVASFFKKFQK-UHFFFAOYSA-N 1-phenylpyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=CC=C1 JMVIVASFFKKFQK-UHFFFAOYSA-N 0.000 description 3
- 150000001409 amidines Chemical class 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- QKSLLUAHJIQQGI-UHFFFAOYSA-N 1-(3-bromophenyl)pyrrolidin-2-one Chemical compound BrC1=CC=CC(N2C(CCC2)=O)=C1 QKSLLUAHJIQQGI-UHFFFAOYSA-N 0.000 description 2
- YINFEFUSAQRZGG-UHFFFAOYSA-N 1-(4-bromophenyl)pyrrolidin-2-one Chemical compound C1=CC(Br)=CC=C1N1C(=O)CCC1 YINFEFUSAQRZGG-UHFFFAOYSA-N 0.000 description 2
- NAIVIVMHCDWBEF-UHFFFAOYSA-N 1-(4-chlorophenyl)pyrrolidin-2-one Chemical compound C1=CC(Cl)=CC=C1N1C(=O)CCC1 NAIVIVMHCDWBEF-UHFFFAOYSA-N 0.000 description 2
- SZZJBOHBVUOQFP-UHFFFAOYSA-N 1-(4-fluorophenyl)pyrrolidin-2-one Chemical compound C1=CC(F)=CC=C1N1C(=O)CCC1 SZZJBOHBVUOQFP-UHFFFAOYSA-N 0.000 description 2
- IDJCCRRYIMWLSQ-UHFFFAOYSA-N 1-(4-methoxyphenyl)pyrrolidin-2-one Chemical compound C1=CC(OC)=CC=C1N1C(=O)CCC1 IDJCCRRYIMWLSQ-UHFFFAOYSA-N 0.000 description 2
- ORPHOKOVVUFNKE-UHFFFAOYSA-N 1-(4-methylphenyl)pyrrolidin-2-one Chemical compound C1=CC(C)=CC=C1N1C(=O)CCC1 ORPHOKOVVUFNKE-UHFFFAOYSA-N 0.000 description 2
- YYYMDBUHBOEDTC-UHFFFAOYSA-N 1-(4-nitrophenyl)pyrrolidin-2-one Chemical compound C1=CC([N+](=O)[O-])=CC=C1N1C(=O)CCC1 YYYMDBUHBOEDTC-UHFFFAOYSA-N 0.000 description 2
- KDRONXZNFIQMDV-UHFFFAOYSA-N 1-naphthalen-1-ylpyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=CC2=CC=CC=C12 KDRONXZNFIQMDV-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- BIPUHAHGLJKIPK-UHFFFAOYSA-N dicyclopropylmethanone Chemical compound C1CC1C(=O)C1CC1 BIPUHAHGLJKIPK-UHFFFAOYSA-N 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- GRWPYGBKJYICOO-UHFFFAOYSA-N 2-methylpropan-2-olate;titanium(4+) Chemical compound [Ti+4].CC(C)(C)[O-].CC(C)(C)[O-].CC(C)(C)[O-].CC(C)(C)[O-] GRWPYGBKJYICOO-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical class NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 description 1
- 238000006736 Huisgen cycloaddition reaction Methods 0.000 description 1
- 238000006683 Mannich reaction Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940058303 antinematodal benzimidazole derivative Drugs 0.000 description 1
- 125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 150000001923 cyclic compounds Chemical class 0.000 description 1
- 125000001511 cyclopentyl group Chemical class [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- OOXWYYGXTJLWHA-UHFFFAOYSA-N cyclopropene Chemical compound C1C=C1 OOXWYYGXTJLWHA-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000006575 electron-withdrawing group Chemical group 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
- 235000019439 ethyl acetate Nutrition 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003254 radicals Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- FKZFOHABAHJDIK-UHFFFAOYSA-K trichloroscandium;hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Cl-].[Sc+3] FKZFOHABAHJDIK-UHFFFAOYSA-K 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/24—Oxygen or sulfur atoms
- C07D207/26—2-Pyrrolidones
- C07D207/263—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
- C07D207/267—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to the ring nitrogen atom
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention provides a method for synthesizing N-aryl pyrrolidine-2-ketone by promoting cyclopropyl ring opening with acid, which belongs to the field of organic synthesis, and the method uses N-aryl cyclopropane formamidine and acyl chloride as substrates to react for 6-24h in an HCl gas atmosphere at the temperature of 110-. The synthesis method of the invention only uses cheapCompared with the prior synthesis method, the amidine compound and the acyl chloride derivative used in the method are cheap and easy to obtain, the condition is mild, the reaction has good regioselectivity and yield, the method has wide functional group tolerance, the synthesis step is simple, the reaction condition is mild, the operation is simple and easy, and the reaction yield is simple and easy to implementUp to 88 percent, the reaction substrate is cheap and easy to obtain, and the applicable substrate range is wide.
Description
Technical Field
The invention belongs to the technical field of organic synthesis, and particularly relates to a method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted cyclopropyl ring opening.
Background
Cyclopropane, which can be ring-opened with the aid of releasing strain energy (27.5kcal/mol) due to its large ring tension, is often used as C 3 Building blocks are used for the synthesis of other cyclic compounds. Over the course of many years, a number of methods have been developed to induce cyclopropyl ring opening, such as: the method comprises the following steps that D-A type cyclopropane ring opening is catalyzed by a metal catalyst, one end of a C-C bond of a cyclopropane substrate is an electron-withdrawing group, the other end of the C-C bond of the cyclopropane substrate is an electron-donating group, and the C-C bond of the cyclopropane is activated by the difference of electronic characteristics of substituent groups to promote the occurrence of ring opening reaction; metal-mediated, metal-catalyzed ring opening of cyclopropene, the presence of allyl groups activating cyclopropane; cyclopropylamines have also developed a number of thermal rearrangement ring-opening, transition metal-catalyzed ring-opening, free radical ring-opening strategies, using complexes of scandium trichloride hexahydrate and chiral N, N' -dioxide to catalyze o-phenylenediamine and cyclopropylketone in 1,2, -dichloroethane to synthesize chiral benzimidazole derivatives via highly efficient asymmetric ring-opening/cyclization/reverse mannich reactions, with mild reaction conditions and a broad substrate range and yields of up to 99% (Xia, y.et al.
The existing nickel-catalyzed [3+2] cycloaddition reaction of cyclopropylaldimine and ketene obtains trisubstituted cyclopentane by using Ni (cod)2 as a catalyst and using an azacyclo-carbene ligand with the aid of titanium tert-butoxide and potassium tert-butoxide, and the method can synthesize some substrates that cannot be synthesized by cyclopropyl ketone (Liu, L.et al.org.Lett.,2007,9,3885 one-pot 3887).
Then carrying out ring-opening cyclization reaction of oxa-chain 1, 7-eneyne with cyclopropyl by gold catalysis, wherein IPrAuNTf is used for the reaction 2 The use of a catalyst in dichloromethane at room temperature makes it possible to obtain highly substituted furan derivatives in moderate to good reaction yields (Zang, W.et al.chem.Commun. (Camb),2019,55, 8126-8129).
The ring-opening strategies described above often involve the disadvantages of post-treatment of the metal scrap, the complexity of the preparation of the substrate, the severity of the reaction conditions, some of which use, for example, Ti (OtBu) 4 Additives such as LiCl and tBuOk are used for improving the reactivity and complex ligands are used for improving the stereoselectivity of the reaction, and in order to overcome the defects, a method for inducing the ring opening of cyclopropane in an acidic environment by using amidine as an inducing group is designedThe molecular sieve provides a dry reaction environment, cyclopropyl can be opened under a mild condition without a metal catalyst and a ligand, and compared with the conventional synthesis method, the amidine compound and the acyl chloride derivative used in the method are cheap and easy to obtain, the condition is mild, the reaction has good regioselectivity and yield, and the method has wide functional group tolerance.
Disclosure of Invention
The invention provides a new idea for promoting the ring opening of cyclopropane by taking amidine as an induction group, under the induction of the group, the reaction can promote the ring opening of the cyclopropane by only using cheap HClThe molecular sieve can be used as a drying solvent environment provided by a drying agent to carry out regioselective cyclopropane ring-opening reaction in an acid environment to synthesize N-arylpyrrolidine-2-ketone.
The invention adopts the following technical scheme:
adding N-arylcyclopropane carboxamidine andmolecular sieves, followed by addition of solvent, then acid chloride and capping, displace the HCl gas once. Heating is started to raise the reaction temperature to 110-130 ℃, and the reaction lasts for 6-24 h.
After the reaction was completed, the reaction mixture was returned to room temperature, and the organic solvent was removed by rotary evaporation. And then, carrying out column chromatography purification on the obtained crude product to obtain the final product N-aryl pyrrolidine-2-ketone.
The synthesis of N-arylpyrrolidin-2-ones according to the above method using acid promoted ring opening of cyclopropyl, wherein the N-arylcyclopropanecarboxamidine has the following general formula:
in the general formula R 1 Is any one of an aryl group and a condensed ring aryl group.
According to the above method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl, the acyl chloride in the reaction has the following general formula:
in the general formula R 2 Is an aryl group.
According to the above method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl, the reaction product N-aryl pyrrolidine-2-ketone derivative has the following general formula:
in the general formula, R is any one of aryl, heteroaryl and condensed ring aryl.
According to the method for synthesizing the N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl, the dosage of the acid chloride in the reaction is 1-2 equivalents of the molar quantity of the N-aryl cyclopropane formamidine.
According to the method for synthesizing the N-aryl pyrrolidine-2-ketone by promoting the ring opening of cyclopropyl by acid, the solvent in the reaction is xylene or toluene.
The method for synthesizing N-aryl pyrrolidine-2-ketone by acid-promoted ring opening of cyclopropyl, which is adopted in the reactionThe dosage of the molecular sieve is 80-240 mg.
According to the method for synthesizing N-aryl pyrrolidine-2-ketone by promoting the ring opening of cyclopropyl by acid, the reaction temperature is 110-130 ℃ and the reaction time is 6-24 h.
According to the method for synthesizing the N-aryl pyrrolidine-2-ketone by promoting the ring opening of cyclopropyl by the acid, the reaction atmosphere in the reaction is HCl gas.
Has the advantages that:
the invention designs a method for inducing the ring opening of cyclopropane by using amidine as an inducing group in an acidic environment. The synthesis method of the invention only uses cheapThe molecular sieve provides a dry reaction environment, and ring opening of cyclopropyl can be realized under mild conditions without a metal catalyst and a ligand. Compared with the prior synthesis method, the amidine compound and the acyl chloride derivative used in the method are cheap and easily available, the conditions are mild, the reaction has good regioselectivity and yield, and the method has wide functional group tolerance.
Drawings
FIG. 1 is a scheme for the preparation of N-phenylpyrrolidin-2-one from example 1 1 H NMR spectrum;
FIG. 2 is a drawing showing a preparation process of example 1Preparation of N-phenylpyrrolidin-2-ones 13 CNMR spectrogram;
FIG. 3 is a schematic representation of the preparation of N- (4-chlorophenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 4 is a scheme showing the preparation of N- (4-chlorophenyl) pyrrolidin-2-one 13 C NMR spectrogram;
FIG. 5 is a scheme showing the preparation of N- (4-bromophenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 6 is a scheme showing the preparation of N- (4-bromophenyl) pyrrolidin-2-one 13 C NMR spectrum;
FIG. 7 is a scheme showing the preparation of N- (3-bromophenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 8 is a scheme showing the preparation of N- (3-bromophenyl) pyrrolidin-2-one 13 C NMR spectrum;
FIG. 9 is a scheme showing the preparation of N- (4-fluorophenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 10 is a scheme showing the preparation of N- (4-fluorophenyl) pyrrolidin-2-one 13 C NMR spectrum;
FIG. 11 is a schematic representation of the preparation of N- (4-nitrophenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 12 is a scheme showing the preparation of N- (4-nitrophenyl) pyrrolidin-2-one 13 C NMR spectrogram;
FIG. 13 is a scheme showing the preparation of N- (4-methylphenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 14 is a scheme showing the preparation of N- (4-methylphenyl) pyrrolidin-2-one 13 C NMR spectrum;
FIG. 15 is a scheme showing the preparation of N- (4-methoxyphenyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 16 is a scheme showing the preparation of N- (4-methoxyphenyl) pyrrolidin-2-one 13 C NMR spectrum;
FIG. 17 is a scheme showing the preparation of N- (1-naphthyl) pyrrolidin-2-one 1 H NMR spectrum;
FIG. 18 is a scheme showing the preparation of N- (1-naphthyl) pyrrolidin-2-one 13 C NMR spectrum;
Detailed Description
For a better illustration of the invention, the following examples are given:
example 1
A process for the preparation of N-phenylpyrrolidin-2-ones of the formula:
to a 25ml reaction tube, 16.0mg (0.1mmol) of the substrate N-phenylcyclopropanecarboxamidine was added,molecular sieves 240mg, xylene 1.5mL, followed by benzoyl chloride (0.15mmol), magneton and seal, replace once dried HCl gas and stir in a 130 deg.C oil bath for 12 h. After the reaction is finished, 1mL of 1M HCl solution is added to hydrolyze the imine intermediate, after the hydrolysis is finished, DCM is used for extracting the water phase for three times, the organic phase is concentrated to obtain a crude product, and the crude product is separated and purified by column chromatography to obtain the target product 13.4mg, wherein the yield is 83%. Target product characterization data: white solid (13.3mg, 83% yield) (hexane/EtOAc ═ 2:1as an element.) Mp:65-66 ℃. 1 H NMR(400MHz,CDCl 3 )δ7.64–7.58(m,2H),7.40–7.34(m,2H),7.18–7.11(m,1H),3.87(t,J=7.0Hz,2H),2.62(t,J=8.1Hz,2H),2.16(p,J=7.5Hz,2H). 13 C NMR(100MHz,CDCl 3 )δ174.22,139.42,128.83,124.51,119.97,48.80,32.77,18.05.LRMS(EI):m/z calcd for C 10 H 11 NO[M] + ,161.08;found,161.00。
Claims (9)
2. A method for synthesizing N-aryl pyrrolidine-2-ketone by promoting ring opening of cyclopropyl with acid is characterized by comprising the following steps: the N-arylcyclopropanecarboxamidine has the following general formula:
in the general formula R 1 Is any one of aryl, heteroaryl and condensed ring aryl.
5. A method for synthesizing N-aryl pyrrolidine-2-ketone by promoting ring opening of cyclopropyl with acid is characterized in that: the dosage of the acyl chloride is 1-2 equivalents of the molar quantity of the N-aryl cyclopropane formamidine.
6. A method for synthesizing N-aryl pyrrolidine-2-ketone by promoting ring opening of cyclopropyl with acid is characterized in that: the solvent is xylene or toluene.
8. A method for synthesizing N-aryl pyrrolidine-2-ketone by promoting ring opening of cyclopropyl with acid is characterized in that: the reaction temperature is 110-130 ℃, and the reaction time is 6-24 h.
9. A method for synthesizing N-aryl pyrrolidine-2-ketone by promoting ring opening of cyclopropyl with acid is characterized in that: the reaction atmosphere is HCl gas.
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CN113185521A (en) * | 2021-05-08 | 2021-07-30 | 新乡市润宇新材料科技有限公司 | Method for preparing tetrahydropyrrolo [1,2-a ]1,3, 5-triazine-4-ketone compound by cyclopropyl ring opening |
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CN113185521A (en) * | 2021-05-08 | 2021-07-30 | 新乡市润宇新材料科技有限公司 | Method for preparing tetrahydropyrrolo [1,2-a ]1,3, 5-triazine-4-ketone compound by cyclopropyl ring opening |
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